Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Zimmer Spine

Address:

Cite Mondiale 23 Parvis des Chartrons

Bordeaux

33080

France

Authorised Representative/ UK Responsible Person
Name: Biomet 3i UK Ltd
Address:

1 Glass Wharf Burges Salmon Rep Office

Bristol

BS2 0ZX

England United Kingdom

Code/Term Type

Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Class IIb

Internal spinal fixation system cable crimp sterile Internal spinal fixation system cable crimp sterile Class IIb

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Polymeric spinal interbody fusion cage	Polymeric spinal interbody fusion cage	Class IIb
Internal spinal fixation system cable crimp sterile	Internal spinal fixation system cable crimp sterile	Class IIb